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Discovery of novel thiosemicarbazone derivatives with potent and selective anti-Candida glabrata activity
A series of 21 novel compounds containing a thiosemicarbazone moiety were designed and synthesised based on hit compound 1 from our in-house compound library screening. Most compounds showed potent antifungal activity in vitro against seven common pathogenic fungi. Notably, all compounds showed high...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120463/ https://www.ncbi.nlm.nih.gov/pubmed/37080774 http://dx.doi.org/10.1080/14756366.2023.2202362 |
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author | Li, Xianru Li, Liping Zhang, Haonan Chi, Xiaochen Jiang, Yuanying Ni, Tingjunhong |
author_facet | Li, Xianru Li, Liping Zhang, Haonan Chi, Xiaochen Jiang, Yuanying Ni, Tingjunhong |
author_sort | Li, Xianru |
collection | PubMed |
description | A series of 21 novel compounds containing a thiosemicarbazone moiety were designed and synthesised based on hit compound 1 from our in-house compound library screening. Most compounds showed potent antifungal activity in vitro against seven common pathogenic fungi. Notably, all compounds showed high potency against Candida glabrata 537 (MIC = ≤0.0156-2 µg/mL). Of note, compounds 5j and 5r displayed excellent antifungal activity against Candida krusei 4946 and Candida auris 922. Additionally, compounds 5j and 5r also showed high potency against 15 C. glabrata isolates with MIC values ranging from 0.0625 µg/mL to 4 µg/mL, with compound 5r being slightly superior to 5j. Moreover, compound 5r has certain effect against biofilm formation of C. glabrata. Furthermore, compound 5r has minimal cytotoxicity against HUVECs with an IC(50) value of 15.89 µg/mL and no haemolysis at 64 µg/mL. Taken together, these results suggest that promising lead compound 5r deserves further investigation. |
format | Online Article Text |
id | pubmed-10120463 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-101204632023-04-22 Discovery of novel thiosemicarbazone derivatives with potent and selective anti-Candida glabrata activity Li, Xianru Li, Liping Zhang, Haonan Chi, Xiaochen Jiang, Yuanying Ni, Tingjunhong J Enzyme Inhib Med Chem Research Paper A series of 21 novel compounds containing a thiosemicarbazone moiety were designed and synthesised based on hit compound 1 from our in-house compound library screening. Most compounds showed potent antifungal activity in vitro against seven common pathogenic fungi. Notably, all compounds showed high potency against Candida glabrata 537 (MIC = ≤0.0156-2 µg/mL). Of note, compounds 5j and 5r displayed excellent antifungal activity against Candida krusei 4946 and Candida auris 922. Additionally, compounds 5j and 5r also showed high potency against 15 C. glabrata isolates with MIC values ranging from 0.0625 µg/mL to 4 µg/mL, with compound 5r being slightly superior to 5j. Moreover, compound 5r has certain effect against biofilm formation of C. glabrata. Furthermore, compound 5r has minimal cytotoxicity against HUVECs with an IC(50) value of 15.89 µg/mL and no haemolysis at 64 µg/mL. Taken together, these results suggest that promising lead compound 5r deserves further investigation. Taylor & Francis 2023-04-20 /pmc/articles/PMC10120463/ /pubmed/37080774 http://dx.doi.org/10.1080/14756366.2023.2202362 Text en © 2023 Department of Pharmacy, Shanghai Tenth People's Hospital, School of Medicine, Tongji University. Published by Informa UK Limited, trading as Taylor & Francis Group https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent. |
spellingShingle | Research Paper Li, Xianru Li, Liping Zhang, Haonan Chi, Xiaochen Jiang, Yuanying Ni, Tingjunhong Discovery of novel thiosemicarbazone derivatives with potent and selective anti-Candida glabrata activity |
title | Discovery of novel thiosemicarbazone derivatives with potent and selective anti-Candida glabrata activity |
title_full | Discovery of novel thiosemicarbazone derivatives with potent and selective anti-Candida glabrata activity |
title_fullStr | Discovery of novel thiosemicarbazone derivatives with potent and selective anti-Candida glabrata activity |
title_full_unstemmed | Discovery of novel thiosemicarbazone derivatives with potent and selective anti-Candida glabrata activity |
title_short | Discovery of novel thiosemicarbazone derivatives with potent and selective anti-Candida glabrata activity |
title_sort | discovery of novel thiosemicarbazone derivatives with potent and selective anti-candida glabrata activity |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120463/ https://www.ncbi.nlm.nih.gov/pubmed/37080774 http://dx.doi.org/10.1080/14756366.2023.2202362 |
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